Primary adrenal insufficiency in patients with acquired immunodeficiency syndrome.

被引:0
|
作者
Dore, MX [1 ]
de la Blanchardiere, A [1 ]
Lesprit, P [1 ]
David, F [1 ]
Beressi, JP [1 ]
Fiet, J [1 ]
Sicard, D [1 ]
Decazes, JM [1 ]
机构
[1] Hop St Louis, Serv Malad Infect, F-75475 Paris 10, France
来源
REVUE DE MEDECINE INTERNE | 1998年 / 19卷 / 01期
关键词
primary adrenal insufficiency; AIDS;
D O I
10.1016/S0248-8663(97)83695-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. - Lesions of adrenal glands are common findings at autopsy patients with acquired immunodeficiency syndrome (AIDS). lit contrast the diagnosis of symptomatic adrenal insufficiency is rarely established during the lifetime of these these patients. Patients. - We report four new cases and review the literature. All four patients had full blown AIDS with a mean CD4 cell count of 19 mu/L. One or more opportunistic disease was present at the time of diagnostic: cytomegalovirus retinitis two cases, disseminated Mycobacterium avium infection in two, Kaposi's sarcoma in two and Candida esophagitis in one. Results. - The clinical presentation constantly included fatigue, weight loss, severe orthostatic hypotension and gastrointestinal disturbances. Cutaneous hyperpigmentation was present in three cases. In most cases biological abnormalities were typical, such as hyponatremia, urinary Na/K ratio greater than or equal to 1, and hyperkalemia. Serum cortisol levels were within the range of normal in three cases but response to the cosyntropin challenge was typically impaired in all cases. Clinical and biological manifestations returned to normal in 1 to 3 weeks after initiation of therapy with cortisol, associated to fludrocortisone in three cases. However, 13 months after diagnosis, three patients were dead. Conclusions. - Usually asymptomatic, diagnostic of symptomatic adrenal insufficiency must be suspected even when clinical presentation is atypical because rapid efficiency of hormonal treatment. (C) 1998, Elsevier, Paris.
引用
收藏
页码:23 / 28
页数:6
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